3-propoxyazetidine hydrochloride

98%

Reagent Code: #224920
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CAS Number 897019-55-5

science Other reagents with same CAS 897019-55-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.63 g/mol
Formula C₆H₁₃NO·HCl
badge Registry Numbers
MDL Number MFCD06804557
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring azetidine-based scaffolds. Its propoxy side chain enhances solubility and influences metabolic stability, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in the preparation of kinase inhibitors and central nervous system agents due to its favorable ring strain and binding properties. Also utilized in research settings for building novel heterocyclic compounds with potential biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,900.00
250mg
10-20 days ฿6,610.00
1g
10-20 days ฿18,720.00
5g
10-20 days ฿76,370.00
3-propoxyazetidine hydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring azetidine-based scaffolds. Its propoxy side chain enhances solubility and influences metabolic stability, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in the preparation of kinase inhibitors and central nervous system agents due to its favorable ring strain and binding properties. Also utilized in research sett

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring azetidine-based scaffolds. Its propoxy side chain enhances solubility and influences metabolic stability, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in the preparation of kinase inhibitors and central nervous system agents due to its favorable ring strain and binding properties. Also utilized in research settings for building novel heterocyclic compounds with potential biological activity.

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